WO1998058953A2 - Nouvelles proteines de membrane externe issues de chlamydia pneumoniae - Google Patents

Nouvelles proteines de membrane externe issues de chlamydia pneumoniae Download PDF

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WO1998058953A2
WO1998058953A2 PCT/DK1998/000266 DK9800266W WO9858953A2 WO 1998058953 A2 WO1998058953 A2 WO 1998058953A2 DK 9800266 W DK9800266 W DK 9800266W WO 9858953 A2 WO9858953 A2 WO 9858953A2
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ser
seq
gly
thr
leu
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PCT/DK1998/000266
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WO1998058953A3 (fr
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Svend Birkelund
Gunna Christiansen
Katrine Knudsen
Anna-Sofie Hebsgaard Pedersen
Per Mygind
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Svend Birkelund
Gunna Christiansen
Katrine Knudsen
Madsen Anna Sofie
Per Mygind
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Application filed by Svend Birkelund, Gunna Christiansen, Katrine Knudsen, Madsen Anna Sofie, Per Mygind filed Critical Svend Birkelund
Priority to DE69834194T priority Critical patent/DE69834194T2/de
Priority to US09/446,677 priority patent/US7264941B1/en
Priority to EP98928179A priority patent/EP1007685B1/fr
Priority to CA002294651A priority patent/CA2294651A1/fr
Priority to BR9810288-5A priority patent/BR9810288A/pt
Priority to AU80119/98A priority patent/AU749382B2/en
Priority to JP50361399A priority patent/JP4160640B2/ja
Publication of WO1998058953A2 publication Critical patent/WO1998058953A2/fr
Publication of WO1998058953A3 publication Critical patent/WO1998058953A3/fr
Priority to US11/826,125 priority patent/US20080226679A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/295—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Chlamydiales (O)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/12—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from bacteria
    • C07K16/1203—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from bacteria from Gram-negative bacteria
    • C07K16/125—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from bacteria from Gram-negative bacteria from Chlamydiales (O)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies

Definitions

  • the present invention relates to the identification of members of a gene family from the human respiratory pathogen Chlamydia pneumoniae , encoding surface exposed membrane proteins of a size of approximately 89-101 kDa and of 56-57 kDa, preferably about 89.6-100.3 kDa and about 56.1 kDa.
  • the invention relates to the novel DNA sequences, the deduced amino acid sequences of the corresponding proteins and the use of the DNA sequences and the proteins in diagnosis of infections caused by C. pneumoniae, in pathology, in epidemiology, and as vaccine components.
  • C. pneumoniae is an obligate intracellular bacteria (Christiansen and Birkelund (1992); Grayston et al . (1986)). It has a cell wall structure as Gram negative bacteria with an outer membrane, a periplasmic space, and a cytoplasmic membrane. It is possible to purify the outer membrane from Gram negative bacteria with the detergent sarkosyl . This fraction is named the 'outer membrane complex (OMC) MCaldwell et al. (1981)). The COMC (Chlamydia outer membrane complex) of C.
  • OMC 'outer membrane complex
  • pneumoniae contains four groups of proteins: A high molecular weight protein 98 kDa as determined by SDS-PAGE, a double band of the cysteine rich outer membrane protein 2 (Omp2) protein of 62/60 kDa, the major outer membrane protein (MOMP) of 38 kDa, and the low-molecular weight lipo-protein Omp3 of 12 kDa.
  • the Omp2/Omp3 and MOMP proteins are present in COMC from all Chlamydia species, and these genes have been cloned from both C. trachomatis, C. psi ttaci and C. pneumoniae .
  • the gene encoding 98 kDa protein from C. pneumoniae COMC have not been characterized or cloned.
  • C. pneumoniae is an obligate intra-cellular bacteria belonging to the genus Chlamydia which can be divided into four species: C. trachomatis , C. pneumoniae, C. psi ttaci and C.pecoru ⁇ .. Common for the four species is their obligate intra cellular growth, and that they have a biphasic life cycle, with an extracellular infectious particle (the elementary body, EB) , and an intercellular replicating form (the reticulate body, RB) . In addition the Chlamydia species are characterized by a common lipopolysaccharide (LPS) epitope that is highly immunogenic in human infection.
  • LPS lipopolysaccharide
  • C. psi ttaci is a variable group of animal pathogens where the avian strains can occasionally infect humans and give rise to a severe pneumonia (ornithosis) .
  • the first C. pneumoniae isolate was obtained from an eye infection, but it was classified as a non-typable Chlamydia. Under an epidemic outbreak of pneumonia in Finland it was realized that the patients had a positive reaction in the Chlamydia genus specific test, (the lygranum test) , and the patients showed a titre increase to the untyped Chlamydia isolates.
  • Chlamydia pneumoniae Similar isolates were obtained in an outbreak of upper respiratory tract infections in Seattle, and the Chlamydia isolates were classified as a new species, Chlamydia pneumoniae (Grayston et al . (1989)) . In addition, C. pneumoniae is suggested to be involved in the development of atherosclerotic lesions and for initiating bronchial asthma (Kuo et al . (1995)) . These two conditions are thought to be caused by either chronic infections, by a hypersensitivity reaction, or both.
  • Sero-diagnosis of Chlamydia infections is currently based on either genus specific tests as the Lygranum test and ELISA, measuring the antibodies to LPS, or the more species specific tests where antibodies to purified EBs are measured by microimmuno fluorescence (Micro- IF) (Wang et al . (1970)) .
  • Micro-IF microimmuno fluorescence
  • the micro-IF method is read by microscopy, and in order to ensure correct readings the result must be compared to the results with C.
  • the present invention aims at providing means for efficient diagnosis of infections with Chlamydia pneumoniae as well as the development of effective vaccines against infection with this microorganism.
  • the invention thus relates to species specific diagnostic tests for infection in a mammal, such as a human, with Chlamydia pneumoniae, said tests being based on the detection of antibodies against surface exposed membrane proteins of a size of approximately 89-101 kDa and of 56-57 kDa, preferably of about 89.6-100.3 kDa and about 56.1 kDa (the range in size of the deduced amino acid sequences was from 100.3 to 89.6 except for Ompl3 with the size of 56.1 kDa) , or the detection of nucleic acid fragments encoding such proteins or variants or subsequences thereof .
  • the invention further relates to the amino acid sequences of proteins according to the invention, to variants and subsequences thereof, and to nucleic acid fragments encoding these proteins or variants or subsequences thereof .
  • the present invention further relates to antibodies against proteins according to the invention.
  • the invention also relates to the use of nucleic acid fragments and proteins according to the invention in diagnosis of Chlamydia pneumoniae and vaccines against Chlamydia pneumoniae .
  • C. pneumoniae Prior to the disclosure of the present invention only a very limited number of genes from C. pneumoniae had been sequenced. These were primarily the genes encoding known C. trachomatis homologues: MOMP, Omp2 , Omp3 , Kdo-transferase, the heat shock protein genes GroEl/Es and DnaK, a ribonuclease P homologue and a gene encoding a 76 kDa protein of unknown function. The reason why so few genes have been cloned to date is the very low yield of C. pneumoniae which can be obtained after purification from the host cells. After such purification the DNA must be purified from the EBs, and at this step the C. pneumoniae DNA can easily be contaminated with host cell DNA.
  • Halme et al . (1997) described the presence of human T-cell epitopes in C. pneumoniae proteins of 92-98 kDa. The proteins were eluted from SDS-PAGE of total chlamydia proteins but the identity of the proteins were not determined.
  • mice infected with C. pneumoniae generate antibodies to the proteins identified by the inventors and named Omp4-15, but do not recognize the SDS treated heat denatured antigens normally used for SDS-PAGE and immunoblotting. However, a strong reaction was seen if the antigen was not heat denatured. It is therefore highly likely that if a similar reaction is seen in connection with human infections the antigens of the present invention will be of invaluable use in sero-diagnostic tests and may very likely be used as a vaccine for the prevention of infections .
  • a polyclonal antibody (PAB 150) was obtained which reacted with all the proteins .
  • This antibody was used to identify the genes encoding the 89.6-101.3 kDa and 56.1 kDa proteins in an expression library of C. pneumoniae DNA.
  • a problem in connection with the present invention was that a family comprising a number of similar genes were found in C. pneumoniae . Therefore, a large number of different clones were required to identify clusters of fragments. Only because the rabbit antibody generated by the use of SDS-denatured antigens contained antibodies to a high number of different epitopes positioned on different members of the protein family did the inventors succeed in cloning and sequencing four of the genes.
  • the rest of the full length genes were from 2526 (Omp7) to 2838 (Ompl5) nucleotides.
  • the deduced amino acid sequences revealed putative polypeptides of 89.6 to 100.3 kDa, except for Ompl3 of 56.1 kDa. Alignment of the deduced amino acid sequences showed a maximum identity of 49% (Omp5/Omp9) when all the sequences were compared. Except for 0mpl3 , the lowest homology was to 0mp7 with no more than 34% identity to any of the other amino acid sequences .
  • the scores for Ompl3 was from 29-32% to all the other sequences.
  • SEQ ID Nos . 1 and 2 correspond to Omp4
  • SEQ ID Nos 3 and 4 correspond to Omp5
  • SEQ ID Nos 5 and 6 correspond to Omp6
  • SEQ ID Nos 7 and 8 correspond to Omp7
  • SEQ ID Nos 9 and 10 correspond to Omp8
  • SEQ ID Nos 11 and 12 correspond to Omp9
  • SEQ ID Nos 13 and 14 corresponds to OmplO
  • SEQ ID Nos 15 and 16 corresponds to Ompll
  • SEQ ID Nos 17 and 18 corresponds to Ompl2
  • SEQ ID Nos 19 and 20 corresponds to Ompl3
  • SEQ ID Nos 21 and 22 corresponds to Ompl4
  • SEQ ID Nos 23 and 24 corresponds to Ompl5.
  • Omp 4 has a size of 98.9 kDa
  • Omp5 has an estimated size of 97.2 kDa
  • Omp6 has an estimated size of 100.3 kDa
  • Omp7 has an estimated size of 89.7 kDa
  • Omp8 has an estimated size of 90.0 kDa
  • Omp9 has an estimated size of 96.7 kDa
  • OmplO has an estimated size of 98.4 kDa
  • Ompll has an estimated size of 97.6 kDa
  • Ompl3 has an estimated size of 56.1 kDa
  • Omp 12 and 14 being partial.
  • SEQ ID No 25 is a subsequence of SEQ ID No 3
  • SEQ ID No 26 is a subsequence of SEQ ID No 4
  • SEQ ID No 27 is a subsequence of SEQ ID No 5
  • SEQ ID No 28 is a subsequence of SEQ ID No 6
  • SEQ ID No 29 is a subsequence of SEQ ID No 7
  • SEQ ID No 30 is a subsequence of SEQ ID No 8.
  • Part of the omp proteins were expressed as fusion proteins, and mice polyclonal monospecific antibodies against the proteins were produced. The antibodies reacted with the surface of C. pneumoniae in both immunofluorescence and immunoelectron microscopy.
  • the 89-101 kDa and 56-57 kDa protein family in C. pneumoniae comprises surface exposed outer membrane proteins .
  • This important finding leads to the realization that members of the 89-101 kDa and 56-57 kDa C. pneumoniae protein family are good candidates for the development of a sero diagnostic test for C. pneumoniae, as well as the development of a vaccine against infections with C. pneumoniae based on using these proteins.
  • the proteins may be used as epidemiological markers, and polyclonal monospecific sera against the proteins can be used to detect C. pneumoniae in human tissue or detect C. pneumoniae isolates in tissue culture.
  • genes encoding the 89-101 kDa and 56-57 kDa such as the 89.6-100.3 kDa and 56.1 protein family may be used for the development of a species specific diagnostic test based on nucleic acid detection/amplification.
  • the full length Omp4 was cloned into an expression vector system that allowed expression of the Omp4 polypeptide .
  • This polypeptide was used as antigen for immunization of a rabbit. Since the protein was purified under denaturing condition the antibody did not react with the native surface of C. pneumoniae, but it reacted with a 98 kDa protein in immunoblotting where purified C. pneumoniae EB was used as antigen. Furthermore, the antibody reacted in paraffin embedded sections of lung tissue from experimentally infected mice.
  • a broad aspect of the present invention relates to a species specific diagnostic test for infection of a mammal, such as a human, with Chlamydia pneumoniae, said test comprising detecting in a patient or preferable in a patient sample the presence of antibodies against proteins from the outer membrane of Chlamydia pneumoniae , said proteins being of a molecular weight of 89-101 kDa or 56-57 kDa, or detecting the presence of nucleic acid fragments encoding said outer membrane proteins or fragments thereof .
  • the term "patient sample” should be taken to mean an amount of serum from a patient, such as a human patient, or an amount of plasma from said patient, or an amount of mucosa from said patient, or an amount of tissue from said patient, or an amount of expectorate, forced sputum or a bronchial aspirate, an amount of urine from said patient, or an amount of cerebrospinal fluid from said patient, or an amount of atherosclerotic lesion from said patient, or an amount of mucosal swaps from said patient, or an amount of cells from a tissue culture originating from said patient, or an amount of material which in any way originates from said patient .
  • the in vivo test in a human according to the present invention includes a skin test known in the art such as an intradermal test, e.g similar to a Mantaux test.
  • a skin test known in the art such as an intradermal test, e.g similar to a Mantaux test.
  • he test could be non-invasive, such as a superficial test on the skin, e.g. by use of a plaster
  • 89-101 kDa protein means proteins normally present in the outer membrane of Chlamydia pneumoniae, which in SDS-PAGE can be observed as one or more bands with an apparent molecular weight substantially in the range of 89-101 kDa. From the deduced amino acid sequences the molecular size varies from 89.6 to 100.3 kDa.
  • Preferred embodiments of the present invention relate to species specific diagnostic tests according to the invention, wherein the outer membrane proteins have sequences selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24.
  • variant When used in connection with proteins according to the present invention the term "variant" should be understood as a sequence of amino acids which shows a sequence similarity of less than 100% to one of the proteins of the invention.
  • a variant sequence can be of the same size or it can be of a different size as the sequence it is compared to.
  • a variant will typically show a sequence similarity of preferably at least 50%, preferably at least 60%, more preferably at least 70%, such as at least 80%, e.g. at least 90%, 95% or 98%.
  • sequence similarity in connection with sequences of proteins of the invention means the percentage of identical and conservatively changed amino acid residues (with respect to both position and type) in the proteins of the invention and an aligned protein of equal of different length.
  • sequence identity in connection with sequences of proteins of the invention means the percentage of identical amino acid with respect to both position and type in the proteins of the invention and an aligned protein of equal of different length.
  • subsequences of one of the proteins of the invention meaning a consecutive stretch of amino acid residues taken from SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO : 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22 , or SEQ ID NO : 24.
  • a subsequence will typically comprise at least 100 amino acids, preferably at least 80 amino acids, more preferably at least 70 amino acids, such as 50 amino acids. It might even be as small as 10-50 amino acids, such as 20-40 amino acids, e.g. about 30 amino acids.
  • a subsequence will typically show a sequence homology of at least 50%, preferably at least 60%, more preferably at least 70%, such as at least 80%, e.g. at least 90%, 95% or 98%.
  • Diagnostic tests according to the invention include immunoassays selected from the group consisting of a direct or indirect EIA such as an ELISA, an immunoblot technique such as a Western blot, a radio immuno assay, and any other non-enzyme linked antibody binding assay or procedure such as a fluorescence, agglutination or precipitation reaction, and nephelometry .
  • a direct or indirect EIA such as an ELISA
  • an immunoblot technique such as a Western blot
  • a radio immuno assay such as a radio immuno assay
  • any other non-enzyme linked antibody binding assay or procedure such as a fluorescence, agglutination or precipitation reaction, and nephelometry .
  • a preferred embodiment of the present invention relates to species specific diagnostic tests according to the invention, said test comprising an ELISA, wherein antibodies against the proteins of the invention or fragments thereof are detected in samples .
  • a preferred embodiment of the invention is an ELISA based on detection in samples of antibodies against proteins of the invention.
  • the ELISA may use proteins of the invention, or variants thereof, i.e. the antigen, as coating agent.
  • An ELISA will typically be developed according to standard methods well known in the art, such as methods described in "Antibodies; a laboratory manual", Ed. David Lane Harlow, Cold Spring Habor laboratories (1988) , which is hereby incorporated by reference.
  • Recombinant proteins will be produced using DNA sequences obtained essentially using methods described in the examples below. Such DNA sequences, comprising the entire coding region of each gene in the gene family of the invention, will be cloned into an expression vector from which the deduced protein sequence can be purified. The purified proteins will be analyzed for reactivity in ELISA using both monoclonal and polyclonal antibodies as well as sera from experimentally infected mice and human patient sera. From the experimentally infected mice sera it is known that non-linear epitopes are recognized predominantly. Thus, it is contemplated that different forms of purification schemes known in the art will be used to analyze for the presence of discontinuous epitopes, and to analyze whether the human immune response is also directed against such epitopes.
  • Preferred embodiments of the present invention relate to species specific diagnostic tests according to the invention, wherein the nucleic acid fragments have sequences selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO : 7, SEQ ID NO : 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21, and SEQ ID NO: 23.
  • variant should be understood as a sequence of nucleic acids which shows a sequence homology of less than 100%.
  • a variant sequence can be of the same size or it can be of a different size as the sequence it is compared to.
  • a variant will typically show a sequence homology of at least 50%, preferably at least 60%, more preferably at least 70%, such as at least 80%, e.g. at least 90%, 95% or 98%.
  • sequence homology in connection with nucleic acid fragments of the invention means the percentage of matching nucleic acids (with respect to both position and type) in the nucleic acid fragments of the invention and an aligned nucleic acid fragment of equal or different length.
  • PCR will be performed for each gene on all available C. pneumoniae isolates. This will provide information on the general variability of the genes or nucleic acid fragments of the invention. Variable regions will be sequenced. From patient samples PCR will be used to amplify variable parts of the genes for epidemiology. Non- variable parts will be used for amplification by PCR and analyzed for possible use as a diagnostic test. It is contemplated that if variability is discovered, PCR of variable regions can be used for epidemiology. PCR of non- variable regions can be used as a species specific diagnostic test . Using genes encoding proteins known to be invariable in all known isolates prepared as targets for PCR to genes encoding proteins with unknown function.
  • Particularly preferred embodiments of the present invention relate to diagnostic tests according to the invention, wherein detection of nucleic acid fragments is obtained by using nucleic acid amplification, preferably polymerase chain reaction (PCR) .
  • nucleic acid amplification preferably polymerase chain reaction (PCR) .
  • PCR based test directed at detecting nucleic acid fragments of the invention or variants thereof.
  • a PCR test will typically be developed according to methods well known in the art and will typically comprise a PCR test capable of detecting and differentiating between nucleic acid fragments of the invention. Preferred are quantitative competitive PCR tests or nested PCR tests.
  • the PCR test according to the invention will typically be developed according to methods described in detail in EP B 540 588, EP A 586 112, EP A 643 140 OR EP A 669 401, which are hereby incorporated by reference.
  • variants and subsequences of one of the nucleic acid fragments of the invention meaning a consecutive stretch of nucleic acids taken from SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 19, SEQ ID NO: 21, or SEQ ID NO: 23.
  • a variant or subsequence will preferably comprise at least 100 nucleic acids, preferably at least 80 nucleic acids, more preferably at least 70 nucleic acids, such as at least 50 nucleic acids. It might even be as small as 10-50 nucleic acids, such as 20-40 nucleic acids, e.g.
  • a subsequence will typically show a sequence homology of at least 30%, preferably at least 60%, more preferably at least 70%, such as at least 80%, e.g. at least 90%, 95% or 98%. The shorter the subsequence, the higher the required homology.
  • a subsequence of 100 nucleic acids or lower must show a homology of at least 80%.
  • a very important aspect of the present invention relates to proteins of the invention derived from Chlamydia pneumoniae having amino acid sequences selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO : 20, SEQ ID NO: 22, and SEQ ID NO: 24 having a sequence similarity of at least 50%, preferably at least 60%, more preferably at least 70%, such as at least 80%, e.g. at least 90%, 95% or 98% and a similar biological function.
  • similar biological function is meant that the protein shows characteristics similar with the proteins derivable from the membrane proteins of Chlamydia pneumoniae .
  • Such proteins comprise repeated motifs of GGAI (at least 2, preferable at least 3 repeats) and/or conserved positions of tryptophan, (w) .
  • Comparison of the DNA sequences from genes encoding Omp4-15 shows that the overall similarity between the individual genes ranges between 43-55%.
  • Comparison of the amino acid sequences of Omp4-15 shows 34-49% identity and 53-64% similarity.
  • the homology is generally scattered along the entire length of the deduced amino acids. However, as seen from figure 8 A - J there are some regions in which the homology is more pronounced. This is seen in the repeated sequence where the sequence GGAI is repeated 4-7 times in the genes. It is interesting that the DNA homology is not conserved for the sequences encoding the four amino acids GGAI. This may indicate a functional role of this part of the protein and indicates that the repeated structure did not occur by a duplication of the gene .
  • GGAI a region from amino acid 400 to 490 has a higher degree of homology than the rest of the protein, with the conserved sequence FYDPI occurring in all sequences.
  • the amino acid tryptophan (W) is perfectly conserved at 4-6 localizations in the C-terminal part of the protein.
  • Preferred embodiments of the present invention relate to polypeptides which comprise subsequences of the proteins of the invention, said subsequences comprising the sequence GGAI . Further preferred embodiments of the present invention relate to polypeptides which comprise subsequences of the proteins of the invention, said subsequences comprising the sequence FSGE .
  • Polypeptides according to the invention will typically be of a length of at least 6 amino acids, preferably at least 15 amino acids, preferably at least 20 amino acids, preferably at least 25 amino acids, preferably at least 30 amino acids, preferably at least 35 amino acids, preferably at least 40 amino acids, preferably at least 45 amino acids, preferably at least 50 amino acids, preferably at least 55 amino acids, preferably at least 100 amino acids.
  • a very important aspect of the present invention relates to nucleic acid fragments of the invention derived from Chlamydia pneumoniae, variants and subsequences thereof.
  • Another important aspect of the present invention relates to antibodies against the proteins according to the invention, such antibodies including polyclonal monospecific antibodies and monoclonal antibodies against proteins with sequences selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 3, SEQ ID NO: 2
  • SEQ ID NO: 4 SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24.
  • kits for the diagnosis of infection of a mammal such as a human, with Chlamydia pneumoniae
  • said kits comprising one or more proteins with amino acid sequences selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24.
  • kits for the diagnosis of infection of a mammal such as a human, with Chlamydia pneumoniae
  • said kits comprising antibodies against a protein with an amino acid sequence selected from the group consisting of SEQ ID NO: 2, SEQ ID NO : 4, SEQ ID NO: 6, SEQ ID NO : 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24.
  • Antibodies included in a diagnostic kit according to the invention can be polyclonal or monoclonal or a mixture hereof .
  • kits for the diagnosis of infection of a mammal such as a human, with Chlamydia pneumoniae
  • said kits comprising one or more nucleic acid fragments with sequences selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO : 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21, and SEQ ID NO: 23.
  • An aspect of the present invention relates to a composition for immunizing a mammal, such as a human, against Chlamydia pneumoniae, said composition comprising one or more proteins with amino acid sequences selected from the group consisting Of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO : 6, SEQ ID NO : 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24.
  • proteins of the invention in prevention of infection of a mammal, such as a human, with C. pneumoniae are important roles for the proteins of the invention in prevention of infection of a mammal, such as a human, with C. pneumoniae.
  • proteins of the invention including variants and subsequences will be produced, typically by using recombinant techniques, and will then be used as an antigen in immunization of mammals, such as rabbits.
  • the hyper immune sera obtained by the immunization will be analyzed for protection against C. pneumoniae infection using a tissue culture assay.
  • monoclonal antibodies will be produced, typically using standard hybridoma techniques, and analyzed for protection against infection with C. pneumoniae .
  • proteins of the invention which will comprise subsequences of said proteins. It is preferred to use polypeptides comprising such subsequences of the proteins of the invention in immunizing a mammal, such as a human, against Chlamydia pneumoniae .
  • An important aspect of the present invention relates to the use of proteins with sequences selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24 in diagnosis of infection of a mammal, such as a human, with Chlamydia pneumoniae .
  • a preferred embodiment of the present invention relates to the use of proteins according to the invention in an undenatured form, in diagnosis of infection of a mammal, such as a human, with Chlamydia pneumoniae .
  • a very important aspect of the present invention relates to the use of proteins with sequences selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 20, SEQ ID NO: 22, and SEQ ID NO: 24, for immunizing a mammal, such as a human, against Chlamydia pneumoniae .
  • a preferred embodiment of the present invention relates to the use of proteins according to the invention in an undenatured form, for immunizing a mammal, such as a human, against Chlamydia pneumoniae .
  • a very important aspect of the present invention relates to the use of nucleic acid fragments with nucleotide sequences selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO : 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 19, SEQ ID NO: 21, and SEQ ID NO: 23 for immunizing a mammal, such as a human, against Chlamydia pneumoniae . It is envisioned that one type of vaccine against C. pneumoniae will be developed by using gene-gun vaccination of mice.
  • nucleic acid fragments typically, different genetic constructs containing nucleic acid fragments, combinations of nucleic acid fragments according to the invention will be used in the gene-gun approach. The mice will then subsequently be analyzed for production of both humoral and cellular immune response and for protection against infection with C. pneumoniae after challenge herewith.
  • the invention also relates to the uses of the proteins of the invention as a pharmaceutical (a vaccine) as well as to the uses thereof for the preparation of a vaccine against infections with Chlamydia pneumoniae .
  • vaccines which contain protein sequences as active ingredients are generally well understood in the art, as exemplified by U.S. Patents 4,608,251; 4,601,903; 4,599,231; 4,599,230; 4,596,792; and 4 , 578 , 770 , all incorporated herein by reference.
  • such vaccines are prepared as injectables either as liquid solutions or suspen- sions; solid forms suitable for solution in, or suspension in, liquid prior to injection may also be prepared.
  • the preparation may also be emulsified.
  • the active immunogenic ingredient is often mixed with excipients which are pharmaceutically acceptable and compatible with the active ingredi- ent .
  • Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like, and combinations thereof.
  • the vaccine may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents, or adjuvants which enhance the effectiveness of the vaccines.
  • the vaccines are conventionally administered parenterally, by injection, for example, either subcutaneously or intramuscularly.
  • Additional formulations which are suitable for other modes of administration include suppositories and, in some cases, oral formulations. These compositions take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations or powders and contain 10-95% of active ingredient, preferably 25-70%, and optionally a suitable carrier .
  • the protein sequences may be formulated into the vaccine as neutral or salt forms known in the art .
  • the vaccines are administered in a manner compatible with the dosage formulation, and in such amount as will be therapeutically effective and immunogenic.
  • the quantity to be administered depends on the subject to be treated. Suitable dosage ranges are of the order of several hundred micrograms active ingredient per vaccination with a preferred range from about 0.1 ⁇ g to 1000 ⁇ g .
  • the immune response may be enhanced if the vaccine further comprises an adjuvant substance as known in the art.
  • Other possibilities involve the use of immunomodulating substances such as lymphokines (e.g. IFN-7, IL-2 and IL-12) or synthetic IFN-7 inducers such as poly I:C in combination with the above-mentioned adjuvants.
  • a living vaccine by introdu- cing, into a non-pathogenic microorganism, at least one nucleic acid fragment encoding a protein fragment or protein of the invention, and effecting expression of the protein fragment or the protein on the surface of the microorganism (e.g. in the form of a fusion protein including a membrane anchoring part or in the form of a slightly modified protein or protein fragment carrying a lipidation signal which allows anchoring in the membrane) .
  • a fusion protein including a membrane anchoring part or in the form of a slightly modified protein or protein fragment carrying a lipidation signal which allows anchoring in the membrane
  • the skilled person will know how to adapt relevant expression systems for this purpose .
  • Another part of the invention is based on the fact that recent research have revealed that a DNA fragment cloned in a vector which is non-replicative in eukaryotic cells may be introduced into an animal (including a human being) by e.g. intramuscular injection or percutaneous administration (the so-called "gene gun” approach) .
  • the DNA is taken up by e.g. muscle cells and the gene of interest is expressed by a promoter which is functioning in eukaryotes, e.g. a viral promoter, and the gene product thereafter stimulates the immune system.
  • a nucleic acid fragment encoding a protein or protein of the invention may be used for effecting in vivo expression of antigens, i.e. the nucleic acid fragments may be used in so-called DNA vaccines.
  • the invention also relates to a vaccine comprising a nucleic acid fragment encoding a protein fragment or a protein of the invention, the vaccine effecting in vivo expression of antigen by an mammal, such as a human, to whom the vaccine has been administered, the amount of expressed antigen being effective to confer substantially increased resistance to infections with Chlamydia pneumoniae in an mammal, such as a human.
  • the efficacy of such a "DNA vaccine” can possibly be enhanced by administering the gene encoding the expression product together with a DNA fragment encoding a protein which has the capability of modulating an immune response.
  • a gene encoding lymphokine precursors or lymphokines e.g. IFN- ⁇ , IL-2, or IL-12
  • lymphokines could be administered together with the gene encoding the immunogenic protein fragment or protein, either by administering two separate DNA fragments or by administering both DNA fragments included in the same vector.
  • DNA fragments comprising a multitude of nucleotide sequences which each encode relevant epitopes of the protein fragments and proteins disclosed herein so as to effect a continuous sensitization of the immune system with a broad spectrum of these epitopes .
  • Figure 1 The figure shows electron microscopy of negative stained purified C. pneumoniae EB (A) and purified OMC (B) .
  • Figure 2 The figure shows silver stained 15% SDS-PAGE of purified EB and OMC. Lane 1, purified C. pneumoniae EB; lane 2, C. pneumoniae OMC; lane 3, purified C. trachomatis EB; and lane 4 C. trachomatis OMC.
  • FIG. 3 The figure shows immunoblotting of C. pneumoniae EB separated by 10% SDS-PAGE, transferred to nitrocellulose and reacted with rabbit anti C. pneumoniae OMC.
  • FIG. 4 The figure shows coomassie blue stained 7.5% SDS-PAGE of recombinant pEX that were detected by the rabbit anti C. pneumoniae serum. Arrow indicated the localization of the 117 kDa b-galactosidase protein.
  • Figure 5 The figure shows immunoblotting of recombinant pEX colones detected by colony blotting separated by 7.5% SDS-PAGE and transferred to nitrocellulose and reacted with rabbit anti C. pneumoniae OMC. Lane 1, seablue molecular weight standard. Lane 2-6 pEX clones cultivated at 42 °C to induce the production of the b-galactosidase fusion proteins.
  • FIG. 6 The figure shows sequence strategy for Omp4 and Omp5. Arrows indicates primers used for sequencing.
  • FIG. 7 C pneumoniae omp genes .
  • the genes are arranged in two clusters. In cluster 1 Ompl2, 11, 10, 5, 4, 13, and 14 are found. In cluster 2 are found Omp6, 7, 8, 9, and 15.
  • FIG. 8 A - J The figure shows alignment of C. pneumoniae Omp4-15, using the program pileup in the GCG package.
  • FIG. 9 The figure shows immunofluorescence of C. pneumoniae infected HeLa, 72 hrs . after infection, reacted with mouse monospecific anti -serum against pEX3-36 fusion protein.
  • pEX3-36 is a part of the 0mp5 gene.
  • FIG. 10 The figure shows immunoblotting of C. pneumoniae EB, lane 1-3 heated to 100°C in SDS-sample buffer, lane 4-6 unheated. Lane 1 reacted with rabbit anti C. pneumoniae OMC; lane 2 and 4 pre-serum; lane 3 and 5 polyclonal rabbit anti pEXl-1 fusion protein; lane 6 MAb 26.1.
  • FIG. 11 The figure shows immunoblotting of C. pneumoniae EB, lane 1-4 heated to lOOoC in SDS-sample buffer, lane 5-6 unheated. Reacted with serum from C57 -black mice 14 days after infection with 10 7 CFU of C. pneumoniae . Lane 1 and 5 mouse 1; lane 2 and 6 mouse 2; lane 3 and 5 mouse 3; and lane 4 and 8 mouse 4.
  • FIG. 12 The figure shows immunohistochemistry analysis of mouse lung tissue with C. pneumoniae inclusions present both in the bronchial epithelium and in the lung parenchyma (arrows) .
  • C. pneumoniae was cultivated in HeLa cells. Cultivation was done according to the specifications of Miyashita and Matsumoto (1992) , with the modification that centrifugation of supernatant and of the later precipitate and turbid bottom layer was carried out at 100,000 X g.
  • the medium was changed to medium that in addition contained 1 mg per ml of cycloheximide .
  • a coverslip was removed from the cultures and the inclusion was tested with an antibody specific for C. pneumoniae (MAb 26.1) (Christiansen et al . 1994) and a monoclonal antibody specific for the species C. trachomatis (MAb 32.3, Loke diagnostics, Arhus Denmark) to ensure that no contamination with C. trachomatis had occurred.
  • the HeLa cells were tested by Hoechst stain for Mycoplasma contamination as well as by culture in BEa and BEg medium (Freund et al . , 1979) . Also the C.
  • pneumoniae stocks were also tested for Mycoplasma contamination by cultivation in BEa and BEg medium. No contamination with C. trachomatis, Mycoplasmas or bacteria were detected in cultures or cells. 72 hours post-infection the monolayer was washed in PBS, the cells were loosened in PBS with a rubber policeman, and the Chlamydia were liberated from the host cell by sonication.
  • the C. pneumoniae EBs and RBs were purified on discontinuous density gradients (Miyashita et al . (1992)). The purity of the Chlamydia EBs were verified by negative staining and electronmicroscopy (Figure 1), only particles of a size of 0.3 to 0.5 mm were detected in agreement with the structure of C.
  • the purified Chlamydia EBs were subjected to sarkosyl extraction as described by Caldwell et al (1981) with the modification that a brief sonication was used to suspend the COMC.
  • the purified COMC was tested by electronmicroscopy and negative staining (Figure 1) , where a folded outer membrane complex was seen.
  • the proteins from purified EBs and C. pneumoniae OMC were separated on 15% SDS-polyacrylamide gel, and the gel was silver stained ( Figure 2) , in lane 1 it is seen that the purified EBs contain major proteins of 100/95 kDa and a protein of 38 kDa, in the purified COMC (lane 2) these two protein groups are also dominant. In addition, proteins with a molecular weight of 62/60 kDa, 55 kDa, and 12 kDa have been enriched in the COMC preparation. When the purified C. pneumoniae EBs are compared to purified C. trachomatis EB (lane 3) it is seen that predominant protein in the C.
  • trachomatis EB is the major outer membrane protein (MOMP) , and it is also the dominant band in the COMC preparation of C. trachomatis (lane 4) , and Omp2 of 60/62 kDa as well as Omp3 at 12 kDa are seen in the preparation. However, no major bands with a size of 100/95 kDa are detected as in the C. pneumoniae COMC preparation.
  • MOMP major outer membrane protein
  • COMC antigen was dissolved in 20 ⁇ l of SDS sample buffer and thereafter divided into 5 vials.
  • the dissolved antigen was further diluted in one ml of PBS and one ml of Freund incomplete adjuvant (Difco laboratories, USA cat. No. 0639-60-6) and injected into the quadriceps muscle of a New Zealand white rabbit.
  • the rabbit was given three times intramuscular injections at an interval of one week, and after further three weeks the dissolved COMC protein, diluted in one ml PBS was injected intravenously, and the procedure was repeated two weeks later.
  • the serum was obtained from the rabbit.
  • Purified C. pneumoniae EBs were separated by SDS-PAGE, and the proteins were electrotransferred to nitrocellulose membrane. The membrane was blocked and immunostained with the polyclonal COMC antibody ( Figure 3) .
  • the serum recognized proteins with a size of 100/95, 60 and 38 kDa in the EB preparation. This is in agreement with the sizes of the outer membrane proteins.
  • C. pneumoniae DNA Due to the cultivation of C. pneumoniae in HeLa cells, contaminating host cell DNA could be present in the EB preparations. Therefore, the purified EB preparations were treated with DNAse to remove contaminating DNA. The C. pneumoniae DNA was then purified by CsCl gradient centrifugation. The C. pneumoniae DNA was partially digested with Sau3A and the fractions containing DNA fragments with a size of approx. 0.5 to 4.0 kb were cloned into the expression vector system pEX (Boehringer, Germany cat. No. 1034 766, 1034 774, 1034 782) .
  • the pEX vector system has a jS-galactosidase gene with multiple cloning sites in the 3 ' end of the /3-galactosidase gene. Expression of the gene is regulated by the PR promoter, so the protein expression can be induced by elevating the temperature from 32 to 42°C. The colonies of recombinant bacteria were transferred to nitrocellulose membranes, and the temperature was increased to 42°C for two hours. The bacteria were lysed by placing the nitrocellulose membranes on filters soaked in 5% SDS. The colonies expressing outer membrane proteins were detected with the polyclonal antibody raised against C. pneumoniae COMC. The positive clones were cultivated in suspension and induced at 42°C for two hours.
  • the protein profile of the clones were analysed by SDS-PAGE, and increases in the size of the induced b-galactosidase were observed ( Figure 4) .
  • the proteins were electrotransferred to nitrocellulose membranes, and the reaction with the polyclonal serum against COMC was confirmed ( Figure 5) .
  • C. pneumoniae DNA was totally digested with BamHI restriction enzyme, and the fragments were cloned into the vector pBluescript.
  • the ligated DNA was electrotransformed into E. coli XLl-Blue and selected on plates containing Ampicillin.
  • the recombinant bacterial colonies were transferred to a nitrocellulose membrane, and colony hybridisation was performed using the inserts of pEX 1-1 clone as a probe.
  • a clone containing a single BamHI fragment of 4.5 kb was found, and the hybridisation to the probe was confirmed by Southern blotting.
  • the insert of the clone was sequenced bi-directionally using synthetic primers for approx. each 300 bp .
  • Omp4 and 0mp5 were transcribed in opposite directions . Downstream 0mp4 a possible termination structure was located. The 3 ' end of the 0mp5 gene was not cloned due to the presence of the BamHI restriction enzyme site positioned within the gene.
  • the two genes had an amino acid identity of 41% (similarity 61%) , and a possible cleavage site for signal peptidase 1 was present at amino acid 17 in Omp4 and amino acid 25 in Omp5.
  • amino acid sequence encoded by two other pEX clones were compared to the sequence of 0mp4 and 0mp5 they also had amino acid homology to the genes. It is seen that the two clones have homology to the same area in the 0mp4 and Omp5 proteins. Consequently, the pEX clones must have originated from two additional genes . Therefore these genes were named Omp6 and Omp7. Similar analyses were performed with the other genes. In contrast to what was seen for Omp4 and 5 none of the other putative omp proteins had a cleavage site for signal peptides.
  • the Omp4 gene was amplified by PCR with primers that contained LIC-sites, and the PCR product was cloned into the pET-30 LIC vector (Novagen) .
  • the histidine tagged fusion protein was expressed by induction of the synthesis by IPTG and purified over a nickel column.
  • the purified Omp4 protein was used for immunization of a rabbit (six times, 8 ⁇ g each time) .
  • the lungs of C. pneumoniae infected mice were obtained three days after intranasal infection.
  • the tissue samples were fixed in 4% formaldehyde, paraffin embedded, sectioned and deparaffinized prior to staining.
  • the sections were incubated with the rabbit serum diluted 1:200 in TBS ( 150 mM NaCl, 20mM Tris pH 7.5) for 30 min at room temperature. After wash two times in TBS the sections were incubated with the secondary antibody (biotinylated goat anti-rabbit antibodies) diluted 1:300 in TBS, followed by two times wash in TBS.
  • the sections were stained with streptavidin-biotin complex (streptABComplex/AP, Dako) for 30 min washed and developed under microscopic inspection with chromagen + new fuchsin
  • the insert of pEXl-1 clone was amplified by PCR using primers containing LIC sites .
  • the PCR product could therefore be inserted in the pET-32 LIC vector (Novagen, UK cat No. 69076- LO OO to t H H
  • mice Due to the realization of the altered migration of the 0mp4-7 proteins without boiling, we chose to analyse antibodies against C. pneumoniae EBs after an experimental infection of mice.
  • C. pneumoniae C57 black mice were inoculated intranasally with 10 7 CFI of C. pneumoniae under a light ether anaesthesia. After 14 days of infection the serum samples were obtained and the lungs were analysed for pathological changes . In two of the mice a severe pneumonia was observed in the lung sections, and in the third mouse only minor changes were observed.
  • the serum from the mice was diluted 1:100 and reacted with purified EBs dissolved in sample buffer with and without boiling.
  • the amino acid homologies were in the range of 51-63%. It is seen that the C. pneumoniae Omp4-5 proteins are most related to the 98 kDa POMP protein of C. psi ttaci . Interestingly, the 98 kDa C. psi ttaci POMP protein is more related to the C. pneumoniae genes than to the other C. psi ttaci genes. The repeated sequences of GGAI were conserved in the 98 kDa POMP protein, but only three GGAI repeats were present in the 90 and 91 kDa C. psi ttaci POMP proteins. For C. psi ttaci it has been shown that antibodies to these proteins seem to be protective for the infection.
  • GTA GTT GCT GGG AAT TTT TCT ACT GCA GAT GGT GGA GCT ATC AAA GGA 711 Val Val Ala Gly Asn Phe Ser Thr Ala Asp Gly Gly Ala He Lys Gly 155 160 165
  • GGT GGC GCC ATC CAT GCT AAA AAG CTA GCC CTT TCC TCT GGA GGC TTT 1095 Gly Gly Ala He His Ala Lys Lys Leu Ala Leu Ser Ser Gly Gly Phe 285 290 295
  • GTT GGT ACC AAA CTC CGA TT CTAGATTGCT AAAACTCCCT AGTTCTTCTA GGGAG 3022 Val Gly Thr Lys Leu Arg Phe 925
  • MOLECULE TYPE protein
  • FRAGMENT TYPE internal
  • TTTTTCTACG ATCCGATTAC TGCTAATACG GCTGCGGATT CTACAGATAC TTTAAATCTC 1200
  • CTCTATTCAA AAAATGCACT TATGCTCTTA AACAATTATG TAGTGCGTTT TGAACAAAAC 480
  • CTTCCCACTT CAGGAAGTAG TACTCCAGTT CCTATTGTGA CTTTCTCTGA CAATAAACAG 840
  • AAAAACTTTT CAACGGATAA TGGCGGTGCT ATCACCGCAA
  • ATTAGCTCTC TCCATTATCT TATGGAGACT GCAAACGAAG GGTTGCAGGG AGACCGTGCT 1920
  • GACTGCCAAG ATGCAACGTA CAATCTAACT CTTGGTTATA CTGTGGATCT TGTTCGTAGT 2580

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Abstract

L'invention concerne l'identification de membres d'une famille génique issue de l'agent pathogène humain des voies respiratoires, Chlamydia pneumoniae, qui codent des protéines membranaires externes présentant une taille d'environ 89 à 101 kDa et 56 à 57 kDa ou, de préférence, une taille d'environ 89,6 à 100,3 kDa et 56,1 kDa. L'invention concerne les nouvelles séquences d'ADN, les séquences aminoacides dérivées des protéines correspondantes, et l'utilisation en pathologie et en épidémiologie de ces séquences d'ADN et de ces protéines pour dépister des infections causées par C. pneumoniae, ou leur utilisation comme substances vaccinales.
PCT/DK1998/000266 1997-06-23 1998-06-19 Nouvelles proteines de membrane externe issues de chlamydia pneumoniae WO1998058953A2 (fr)

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DE69834194T DE69834194T2 (de) 1997-06-23 1998-06-19 Oberfläche-exponierte proteine von chlamydia pneumoniae
US09/446,677 US7264941B1 (en) 1997-06-23 1998-06-19 Surface exposed proteins from Chlamydia pneumoniae
EP98928179A EP1007685B1 (fr) 1997-06-23 1998-06-19 Nouvelles proteines de membrane externe issues de chlamydia pneumoniae
CA002294651A CA2294651A1 (fr) 1997-06-23 1998-06-19 Nouvelles proteines de membrane externe issues de chlamydia pneumoniae
BR9810288-5A BR9810288A (pt) 1997-06-23 1998-06-19 Teste diagnóstico especìfico para espécie para identificar infecção de um mamìfero, como um humano, com chlamydia pneumoniae, fragmento de ácido nucleico derivado de chlamydia pneumoniae, proteìna derivada de chlamydia pneumoniae, anticorpo monoespecìfico policlonal, kit diagnóstico para o diagnóstico de infecção de um mamìfero, como um humano, com chlamydia pneumoniae, composição para imunizar um mamìfero comoum humano, contra chlamydia pneumoniae, uso de uma proteìna, e, uso de um fragmento de ácido nucleico.
AU80119/98A AU749382B2 (en) 1997-06-23 1998-06-19 Novel surface exposed proteins from chlamydia pneumoniae
JP50361399A JP4160640B2 (ja) 1997-06-23 1998-06-19 クラミジア・ニューモニエ由来の表面露出タンパク質
US11/826,125 US20080226679A1 (en) 1997-06-23 2007-07-12 Novel surface exposed proteins from chlamydia pneumoniae

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WO2000024902A1 (fr) * 1998-10-28 2000-05-04 Connaught Laboratories Limited Antigenes de $i(chlamydia) et fragments correspondants d'adn ainsi que leurs utilisations
WO2000024765A2 (fr) * 1998-10-28 2000-05-04 Aventis Pasteur Limited Antigenes de chlamydia, fragments d'adn correspondant et leurs utilisations
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WO2001021804A1 (fr) * 1999-09-20 2001-03-29 Aventis Pasteur Limited Antigenes de chlamydia, fragments d'adn correspondants et utilisations
JP2004502415A (ja) * 2000-07-03 2004-01-29 カイロン　エセ．ピー．アー． Ｃｈｌａｍｙｄｉａｐｎｅｕｍｏｎｉａｅに対する免疫化
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US6899880B2 (en) 2000-02-01 2005-05-31 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by chlamydia
US7253275B2 (en) 2002-03-07 2007-08-07 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by Chlamydia

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WO2000024765A3 (fr) * 1998-10-28 2000-11-09 Connaught Lab Antigenes de chlamydia, fragments d'adn correspondant et leurs utilisations
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US6872814B2 (en) * 1998-10-29 2005-03-29 Aventis Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
WO2000026237A3 (fr) * 1998-10-29 2000-09-21 Connaught Lab Antigenes a chlamydia et fragments d'adn correspondants et leurs utilisations
WO2000032794A3 (fr) * 1998-12-01 2000-11-09 Aventis Pasteur Antigenes de chlamydia et fragments d'adn correspondants et leur utilisation
WO2000032784A1 (fr) * 1998-12-01 2000-06-08 Aventis Pasteur Limited Antigenes de chlamydia et fragments d'adn correspondants et leur utilisation
US7736873B2 (en) 1998-12-01 2010-06-15 Sanofi Pasteur Limited Chlamydia polypeptides and corresponding DNA fragments and uses thereof
US7326545B2 (en) 1998-12-01 2008-02-05 Sanofi Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
WO2000032794A2 (fr) * 1998-12-01 2000-06-08 Aventis Pasteur Limited Antigenes de chlamydia et fragments d'adn correspondants et leur utilisation
US7183402B2 (en) 1999-03-12 2007-02-27 Sanofi Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
US7285276B2 (en) 1999-03-12 2007-10-23 Sanofi Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
AU775695B2 (en) * 1999-03-12 2004-08-12 Aventis Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
WO2000055326A1 (fr) * 1999-03-12 2000-09-21 Aventis Pasteur Limited Antigenes $i(chlamydia), fragments d'adn correspondants, et leurs utilisations
US7629327B2 (en) 1999-03-12 2009-12-08 Sanofi Pasteur Limited Chlamydia 60 Kda CRMP antigens and vaccine uses
US7595058B2 (en) 1999-05-03 2009-09-29 Sanofi Pasteur Limited Chlamydia antigens and vaccine uses of the protein
US7070792B2 (en) 1999-05-03 2006-07-04 Sanofi Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
JP2002542827A (ja) * 1999-05-03 2002-12-17 アベンティス、パストゥール、リミテッド クラミジア抗原および対応するｄｎａ断片ならびにその使用
WO2000066739A3 (fr) * 1999-05-03 2001-01-11 Aventis Pasteur Antigenes de chlamydia, fragments d'adn correspondants et utilisation de ceux-ci
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US7314869B2 (en) 1999-09-20 2008-01-01 Sanofi Pasteur Limited Chlamydia antigens and corresponding DNA fragments and uses thereof
JP2003510050A (ja) * 1999-09-20 2003-03-18 アベンティス、パストゥール、リミテッド クラミジア抗原および対応するｄｎａ断片ならびにその使用
US7662391B2 (en) 1999-09-20 2010-02-16 Sanofi Pasteur Limited Chlamydia outer membrane protein (OMP) and vaccine uses of the protein
WO2001021804A1 (fr) * 1999-09-20 2001-03-29 Aventis Pasteur Limited Antigenes de chlamydia, fragments d'adn correspondants et utilisations
US6899880B2 (en) 2000-02-01 2005-05-31 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by chlamydia
US8105607B2 (en) 2000-02-01 2012-01-31 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by Chlamydia
JP2004502415A (ja) * 2000-07-03 2004-01-29 カイロン　エセ．ピー．アー． Ｃｈｌａｍｙｄｉａｐｎｅｕｍｏｎｉａｅに対する免疫化
US7253275B2 (en) 2002-03-07 2007-08-07 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by Chlamydia
US7670855B2 (en) 2002-03-07 2010-03-02 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by Chlamydia
US8025891B2 (en) 2002-03-07 2011-09-27 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by Chlamydia
US8337866B2 (en) 2002-03-07 2012-12-25 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by chlamydia
US8679510B2 (en) 2002-03-07 2014-03-25 The Regents Of The University Of California Porin B (PorB) as a therapeutic target for prevention and treatment of infection by Chlamydia

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DE69834194T2 (de) 2007-03-29
BR9810288A (pt) 2000-09-19
AU8011998A (en) 1999-01-04
CA2294651A1 (fr) 1998-12-30
US20080226679A1 (en) 2008-09-18
US7264941B1 (en) 2007-09-04
DE69834194D1 (de) 2006-05-24
ATE323164T1 (de) 2006-04-15
AU749382B2 (en) 2002-06-27
JP4160640B2 (ja) 2008-10-01
PT1007685E (pt) 2006-08-31
CN1249233C (zh) 2006-04-05
CN1261403A (zh) 2000-07-26
WO1998058953A3 (fr) 1999-03-18
DK1007685T3 (da) 2006-08-14
EP1007685B1 (fr) 2006-04-12
ES2264810T3 (es) 2007-01-16
JP2002510970A (ja) 2002-04-09
EP1007685A2 (fr) 2000-06-14

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